In March 2010, Poly Implant Prothèse (PIP) silicone implants were withdrawn from the European Union (EU) market following an observed increase in implant ruptures, and confirmation of the use of substandard silicone in the manufacture of the implants by French regulator AFSSAPS (Agence Française de Sécurité Sanitaire des Produits de Santé). Regulatory authorities in other jurisdictions were also notified, leading to product withdrawal from a number of non-EU countries. PIP implants have also been sold under the trade name of M-Implants and in April 2010 the Dutch Health Care Inspectorate prohibited all trade and usage of both products in the Netherlands.
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